Does PROPRANOLOL Cause Product use in unapproved indication? 2,210 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,210 reports of Product use in unapproved indication have been filed in association with PROPRANOLOL (Propranolol Hydrochloride). This represents 11.4% of all adverse event reports for PROPRANOLOL.
2,210
Reports of Product use in unapproved indication with PROPRANOLOL
11.4%
of all PROPRANOLOL reports
78
Deaths
327
Hospitalizations
How Dangerous Is Product use in unapproved indication From PROPRANOLOL?
Of the 2,210 reports, 78 (3.5%) resulted in death, 327 (14.8%) required hospitalization, and 90 (4.1%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PROPRANOLOL. However, 2,210 reports have been filed with the FAERS database.
What Other Side Effects Does PROPRANOLOL Cause?
Off label use (5,157)
Drug ineffective (2,510)
Product use issue (2,068)
Toxicity to various agents (1,598)
Completed suicide (1,404)
Hypotension (963)
Product administered to patient of inappropriate age (960)
Bradycardia (934)
Nausea (904)
Drug intolerance (894)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which PROPRANOLOL Alternatives Have Lower Product use in unapproved indication Risk?
PROPRANOLOL vs PROPRANOLOL\PROPRANOLOL
PROPRANOLOL vs PROPYLENE GLYCOL
PROPRANOLOL vs PROPYLTHIOURACIL
PROPRANOLOL vs PROTAMINE
PROPRANOLOL vs PROTHIPENDYL